VitaPrep 2113-0013

GUDID 30808232001243

Plasma Separator

Stryker Corporation

Blood centrifugation system containment kit

• Primary Device ID: 30808232001243
• NIH Device Record Key: d6aa766b-49d9-4310-8f8b-1cd79d10d1c2
• Commercial Distribution Discontinuation: 2018-06-30
• Commercial Distribution Status: Not in Commercial Distribution
• Brand Name: VitaPrep
• Version Model Number: 2113-0013
• Catalog Number: 2113-0013
• Company DUNS: 149183167
• Company Name: Stryker Corporation
• Device Count: 1
• DM Exempt: false
• Pre-market Exempt: false
• MRI Safety Status: Labeling does not contain MRI Safety Information
• Human Cell/Tissue Product: false
• Device Kit: false
• Device Combination Product: true
• Single Use: true
• Lot Batch: true
• Serial Number: false
• Manufacturing Date: false
• Expiration Date: true
• Donation Id Number: false
• Contains Natural Rubber Latex: false
• Labeled No Natural Rubber Latex: true
• RX Perscription: true
• OTC Over-The-Counter: false

Customer Support Contacts

• Phone: +1(610)640-1775
• Email: obxsharedservices@stryker.com
• Phone: +1(610)640-1775
• Email: obxsharedservices@stryker.com

Operating and Storage Conditions

• Storage Environment Temperature: Between 20 Degrees Celsius and 30 Degrees Celsius
• Storage Environment Temperature: Between 20 Degrees Celsius and 30 Degrees Celsius

Device Identifiers

Device Issuing Agency	Device ID
GS1	00808232001242 [Primary]
GS1	30808232001243 [Package]; Contains: 00808232001242; Package: pack [5 Units]; Discontinued: 2018-06-30; Not in Commercial Distribution

FDA Pre-market Approvals/Notifications & deNovo

• Premarket Approval: P050044

FDA Product Code

• LMF: Agent, absorbable hemostatic, collagen based

Sterilization

• Steralize Prior To Use: false
• Device Is Sterile: true

Device Entry Metadata

• Public Version Status: Update
• Device Record Status: Published
• Public Version Number: 3
• Public Version Date: 2019-04-23
• Device Publish Date: 2014-09-24

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